US7893114B2 - Silica-based sols and their production and use - Google Patents

Silica-based sols and their production and use Download PDF

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US7893114B2
US7893114B2 US12/792,419 US79241910A US7893114B2 US 7893114 B2 US7893114 B2 US 7893114B2 US 79241910 A US79241910 A US 79241910A US 7893114 B2 US7893114 B2 US 7893114B2
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aqueous
silica
process according
ion exchange
alkali metal
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US20100236738A1 (en
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Glenn Mankin
Marek Tokarz
Freddie Hansson
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Nouryon Chemicals International BV
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Akzo Nobel NV
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    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/14—Colloidal silica, e.g. dispersions, gels, sols
    • C01B33/141—Preparation of hydrosols or aqueous dispersions
    • C01B33/142—Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates
    • C01B33/143—Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates of aqueous solutions of silicates
    • C01B33/1435—Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates of aqueous solutions of silicates using ion exchangers
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63—Inorganic compounds
    • D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
    • D21H17/68—Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24—Polysaccharides
    • D21H17/28—Starch
    • D21H17/29—Starch cationic
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
    • D21H17/375—Poly(meth)acrylamide
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45—Nitrogen-containing groups
    • D21H17/455—Nitrogen-containing groups comprising tertiary amine or being at least partially quaternised
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/06—Paper forming aids
    • D21H21/10—Retention agents or drainage improvers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/924—Significant dispersive or manipulative operation or step in making or stabilizing colloid system
    • Y10S516/928—Mixing combined with non-mixing operation or step, successively or simultaneously, e.g. heating, cooling, ph change, ageing, milling

Definitions

  • the present invention generally relates to silica-based sols suitable for use in papermaking. More particularly, the invention relates to silica-based sols, their production and use in papermaking. The present invention provides an improved method of producing silica-based sols with high stability and SiO 2 contents as well as improved drainage performance.
  • an aqueous suspension containing cellulosic fibres and optional fillers and additives referred to as stock
  • stock is fed into a headbox which ejects the stock onto a forming wire.
  • Water is drained from the stock so that a wet web of paper is formed on the wire, and the web is further dewatered and dried in the drying section of the paper machine. Drainage and retention aids are conventionally introduced into the stock in order to facilitate drainage and to increase adsorption of fine particles onto the cellulosic fibres so that they are retained with the fibres on the wire.
  • Sols of silica-based particles are widely used as drainage and retention aids in combination with charged organic polymers. Such additive systems are among the most efficient now in use in the papermaking industry.
  • One of the parameters affecting the properties and performance of silica-based sols is the specific surface area; stable, high-performance silica-based sols usually contain particles with a specific surface area of at least 300 m 2 /g.
  • Another parameter is the S value, which indicates the degree of aggregate or microgel formation; a lower S-value is indicative of a higher degree of aggregation.
  • U.S. Pat. No. 5,368,833 discloses a silica sol comprising silica particles having a specific surface area within the range of from 750 to 1,000 m 2 /g which are surface-modified with aluminium to a degree of from 2 to 25% substitution of silicon atoms, and wherein the sol has an S value within the range of from 8 to 45%.
  • Said patent also discloses a process for producing the silica sol which comprises the steps of acidifying a water glass solution to a pH within the range of from 1 to 4; alkalising the acid sol at an SiO 2 content within the range of from 7 to 4.5% by weight; allowing particle growth of the sol to a specific surface area within the range of from 750 to 1,000 m 2 /g; and subjecting the sol to aluminium modification.
  • U.S. Pat. No. 5,603,805 discloses silica sols having an S value within the range of from 15 to 40% comprising anionic silica particles, said silica particles optionally being aluminium modified, and having a specific surface area within the range of from 300 to 700 m 2 /g.
  • Said patent also discloses a process for producing the silica sol comprising the steps of acidifying a water glass solution to a pH within the range of from 1 to 4; alkalising the acid sol at an SiO 2 content within the range of from 7 to 5% by weight; alternatively alkalisation of the acid sol to a pH value between 7 and 9; and particle growth of the sol to a specific surface area within the range of from 300 to 700 m 2 /g; and optionally followed by aluminium modification.
  • WO 98/56715 discloses a process for preparing an aqueous polysilicate microgel which comprises mixing an aqueous solution of an alkali metal silicate with an aqueous phase of a silica-based material having a pH of 11 or less.
  • the polysilicate microgel is used as a flocculating agent in combination with at least one cationic or amphoteric polymer in the production of pulp and paper and for water purification.
  • WO 00/66492 discloses a process for the production of an aqueous sol containing silica-based particles which comprises acidifying an aqueous silicate solution to a pH of from 1 to 4 to form an acid sol; alkalising the acid sol in a first alkalisation step; allowing particle growth of the alkalised sol for at least 10 minutes and/or heat-treating the alkalised sol at a temperature of at least 30° C.; alkalising the obtained sol in a second alkalisation step; and optionally modifying the silica-based sol with, for example, aluminium.
  • U.S. Pat. No. 6,372,806 discloses a process for preparing a stable colloidal silica having an S-value of from 20-50 and wherein said silica has a surface area of greater than 700 m 2 /g comprising: (a) charging a reaction vessel with a cationic ion exchange resin having at least 40 percent of its ion exchange capacity in the hydrogen form wherein said reaction vessel has means for separating said colloidal silica from said ion exchange resin; (b) charging said reaction vessel with an aqueous alkali metal silicate having a mole ratio of SiO 2 to alkali metal oxide in the range of from 15:1 to 1:1 and a pH of at least 10.0; (c) stirring the contents of said reaction vessel until the pH of said contents is in the range of from 8.5 to 11.0; (d) adjusting the pH of the contents of said reaction vessel to above 10.0 using an additional amount of said alkali metal silicate; and (e) separating the resulting colloidal silica from said i
  • U.S. Pat. No. 5,176,891 discloses a method for the production of water soluble polyaluminosilicate microgels having a surface area of at least about 1,000 m 2 /g, comprising the steps of (a) acidifying a dilute solution of alkali metal silicate containing about 0.1 to 6 wt.
  • silica-based sols with high stability and SiO 2 contents as well as improved drainage performance. It would also be advantageous to be able to provide improved processes for the preparation of silica-based sols with stability and SiO 2 contents as well as improved drainage performance. It would also be advantageous to be able to provide a papermaking process with improved drainage.
  • the present invention is generally directed to a process for producing a silica-based sol which comprises:
  • the invention is further generally directed to a process for producing a silica-based sol which comprises:
  • the invention is further directed to a silica-based sol and a silica-based sol obtainable by the processes.
  • the invention is further directed to uses of the silica-based sol according to the invention, in particular as a drainage and retention aid in papermaking and for water purification.
  • the invention is further generally directed to a process for producing paper which comprises
  • silica-based sols which are suitable for use as flocculating agents in water purification and as drainage and retention aids in papermaking.
  • the silica-based sols of the invention exhibit good stability over extended periods of time, notably high surface area stability and high stability to avoid complete gel formation.
  • the silica-based sols further result in very good drainage and retention when used in papermaking, in particular improved drainage.
  • the present invention makes it possible to increase the speed of the paper machine and to use a lower dosage of additive to give a corresponding drainage effect, thereby leading to an improved papermaking process and economic benefits.
  • the silica-based sols of the invention can be prepared by a process that is simple, quick and easy to control and regulate, and the process makes it possible to utilize simple and less expensive production equipment.
  • the silica-sols of the invention can be produced by a process that is simplified, improved and more economic.
  • the ion exchange resin used in the process is cationic and has at least part of its ion exchange capacity in the hydrogen form, i.e. an acid cationic ion exchange resin, preferably a weak acid cationic ion exchange resin.
  • the ion exchange resin has at least 40% of its ion exchange capacity in the hydrogen form, preferably at least 50%.
  • Suitable ion exchange resins are provided on the market by several manufacturers, for example Amberlite® IRC84SP from Rohm & Haas.
  • a reaction vessel equipped with means for mixing, e.g. a stirrer is charged with the ion exchange resin.
  • the ion exchange resin is regenerated by addition of an acid, e.g. sulphuric acid, preferably according to manufacturer's instruction.
  • Step (b) of the process comprises bringing together the cationic ion exchange resin with an aqueous alkali metal silicate.
  • this is achieved by adding the ion exchange resin and aqueous alkali metal silicate to the reaction vessel.
  • a reaction vessel containing regenerated ion exchange resin is charged with the aqueous alkali metal silicate whereby an aqueous slurry is formed.
  • the aqueous alkali metal silicate is added to a reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form at a rate in the range of from 0.5 to 50 g SiO 2 per minute and kg ion exchange resin, calculated as ion exchange resin having 100% of its ion exchange capacity in hydrogen form, suitably from 1 to 35, and preferably from 2 to 20.
  • a reaction vessel containing the aqueous alkali metal silicate is charged with the regenerated ion exchange resin whereby an aqueous slurry is formed.
  • aqueous alkali metal silicates or water glass examples include conventional materials, e.g. lithium, sodium and potassium silicates, preferably sodium silicate.
  • the molar ratio of silica to alkali metal oxide, e.g. SiO 2 to Na 2 O, K 2 O or Li 2 O, or a mixture thereof, in the silicate solution can be in the range of from 15:1 to 1:1, suitably in the range of from 4.5:1 to 1.5:1, preferably from 3.9:1 to 2.5:1.
  • the aqueous alkali metal silicate used can have an SiO 2 content of from about 2 to about 35% by weight, suitably from about 5 to about 30% by weight, and preferably from about 15 to about 25% by weight.
  • the pH of the aqueous alkali metal silicate is usually above 11, typically above 12.
  • Step (c) of the process comprises stirring the aqueous slurry formed in step (b) until the pH of the aqueous phase is in the range of from 5.0 to 8.0.
  • stirring is carried out until the pH of the aqueous phase is in the range of from 6.0 to 8.0, preferably from 6.5 to 7.5.
  • particle growth takes place while stirring the aqueous slurry.
  • the silica-based particles formed usually have a specific surface area of at least 300 m 2 /g, preferably at least 700 m 2 /g.
  • the specific surface area is suitably up to 1,500 m 2 /g, preferably up to 1,000 m 2 /g.
  • the slurry is stirred to allow particle aggregation and microgel formation, usually corresponding to an S value in the range of from 5 to 45%, suitably from 8 to 35%, preferably from 10 to 25% and most preferably from 15 to 23%.
  • the stirring usually takes place during a period of time of from 5 to 240 minutes, preferably from 15 to 120 minutes.
  • Step (c) of the process can be carried out simultaneously with and/or after step (b).
  • the aqueous alkali metal silicate is added under stirring to the reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form and then, after completed addition, the stirring continues to achieve the pH and optionally particle aggregation or microgel formation as described above.
  • the aqueous alkali metal silicate is added under stirring to the reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form to achieve the pH and optionally particle aggregation or microgel formation as described above.
  • Step (d) of the process comprises adding to the aqueous phase one or more materials.
  • the pH of the aqueous phase is suitably adjusted to above 9.0, preferably raised to a pH above 10.0; suitably the pH is in the range of from 9.2 to 11.5, preferably from 9.5 to 11.2, and most preferably from 10.0 to 11.0.
  • at least one alkaline material is added, either singly or in combination with at least one second material.
  • alkaline materials include aqueous alkali metal silicates, e.g. any of those defined above, preferably sodium silicate; aqueous alkali metal hydroxides, e.g. sodium and potassium hydroxides, preferably sodium hydroxide; ammonium hydroxide; alkaline aluminium salts, e.g. aluminates, suitably aqueous aluminates, e.g. sodium and potassium aluminates, preferably sodium aluminate.
  • aqueous alkali metal silicates e.g. any of those defined above, preferably sodium silicate
  • aqueous alkali metal hydroxides e.g. sodium and potassium hydroxides, preferably sodium hydroxide
  • ammonium hydroxide e.g. aluminates
  • alkaline aluminium salts e.g. aluminates, suitably aqueous aluminates, e.g. sodium and potassium aluminates, preferably sodium aluminate.
  • suitable second materials include aluminium compounds and organic nitrogen-containing compounds.
  • suitable aluminium compounds include neutral and essentially neutral aluminium salts, e.g. aluminium nitrate, alkaline aluminium salts, e.g. any of those defined above, preferably sodium aluminate.
  • suitable organic nitrogen-containing compounds include primary amines, secondary amines, tertiary amines and quaternary amines, the latter also referred to as quaternary ammonium compounds.
  • the nitrogen-containing compound is preferably water-soluble or water-dispersible.
  • the amine can be uncharged or cationic.
  • Examples of cationic amines include acid addition salts of primary, secondary and tertiary amines and, preferably, quaternary ammonium compounds, as well as their hydroxides.
  • the organic nitrogen-containing compound usually has a molecular weight below 1,000, suitably below 500 and preferably below 300.
  • a low molecular weight organic nitrogen-containing compound is used, for example those compounds having up to 25 carbon atoms, suitably up to 20 carbon atoms, preferably from 2 to 12 carbon atoms and most preferably from 2 to 8 carbon atoms.
  • the organic nitrogen-containing compound has one or more oxygen-containing substituents, for example with oxygen in the form of hydroxyl groups and/or alkyloxy groups. Examples of preferred substituents of this type include hydroxy alkyl groups, e.g. ethanol groups, and methoxy and ethoxy groups.
  • the organic nitrogen-containing compounds may include one or more nitrogen atoms, preferably one or two.
  • Preferred amines include those having a pKa value of at least 6, suitably at least 7 and preferably at least 7.5.
  • Suitable primary amines i.e. amines having one organic substituent
  • alkyl amines e.g. propyl amine, butyl amine and cyclohexyl amine
  • alkanol amines e.g. ethanol amine
  • alkoxyalkyl amines e.g. 2-methoxyethyl amine
  • suitable secondary amines i.e. amines having two organic substituents, include dialkyl amines, e.g. diethyl amine, dipropyl amine and di-isopropyl amine; dialkanol amines, e.g. diethanol amine, and pyrrolidine.
  • Suitable tertiary amines i.e. amines having three organic substituents
  • suitable quaternary amines, or quaternary ammonium compounds, i.e. amines having four organic substituents include tetraalkanol amines, e.g.
  • N-alkyltrialkanol amines e.g. methyltriethanol ammonium hydroxide and methyltriethanol ammonium chloride
  • N,N-dialkyldialkanol amines e.g. dimethyl diethanol ammonium hydroxide and dimethyl diethanol ammonium chloride
  • N,N,N-trialkyl alkanol amines e.g. choline hydroxide and choline chloride
  • N,N,N-trialkyl benzyl amines e.g.
  • tetraalkyl ammonium salts e.g. tetramethyl ammonium hydroxide, tetramethyl ammonium chloride, tetraethyl ammonium hydroxide, tetraethyl ammonium chloride, tetra-propyl ammonium hydroxide, tetrapropyl ammonium chloride, diethyldimethyl ammonium hydroxide, diethyldimethyl ammonium chloride, triethylmethyl ammonium hydroxide and triethylmethyl ammonium chloride.
  • tetraalkyl ammonium salts e.g. tetramethyl ammonium hydroxide, tetramethyl ammonium chloride, tetraethyl ammonium hydroxide, tetraethyl ammonium chloride, tetra-propyl ammonium hydroxide, tetrapropyl ammonium chloride, diethyldi
  • suitable diamines include aminoalkylalkanol amines, e.g. aminoethylethanol amine, piperazine and nitrogen-substituted piperazines having one or two lower alkyl groups of 1 to 4 carbon atoms.
  • suitable organic nitrogen-containing compounds include triethanol amine, diethanol-amine, dipropyl amine, aminoethyl ethanol amine, 2-methoxyethyl amine, N,N-dimethyl-ethanol amine, choline hydroxide, choline chloride, tetramethyl ammonium hydroxide, tetraethyl ammonium hydroxide and tetraethanol ammonium hydroxide.
  • aqueous alkali metal silicate is added, either singly or in combination with aqueous sodium aluminate or aqueous organic nitrogen-containing compound.
  • the materials can be added in any order, preferably the alkaline material is added first followed by adding the second material.
  • alkali metal silicate e.g. sodium silicate
  • an alkaline aluminium salt e.g. aqueous sodium aluminate
  • aqueous alkali metal hydroxide e.g. sodium hydroxide
  • an alkaline aluminium salt e.g. aqueous sodium aluminate
  • aluminium compound provides an aluminated silica-based sol.
  • the addition of aluminium compound results in aluminium modification of the silica-based particles, preferably the particles are surface-modified by aluminium.
  • the amount of aluminium compound used can be varied within wide limits. Usually the amount of aluminium compound added corresponds to a mole ratio of Si:Al of from 10:1 to 100:1, suitably from 20:1 to 50:1, preferably from 25:1 to 35:1, and most preferably from 25:1 to 30:1.
  • alkali metal silicate e.g. sodium silicate
  • an organic nitrogen-containing compound e.g. aqueous choline hydroxide
  • aqueous alkali metal hydroxide e.g. sodium hydroxide
  • an organic nitrogen-containing compound e.g. aqueous choline hydroxide
  • the addition of organic nitrogen-containing compound provides a nitrogen-modified silica-based sol.
  • the amount of organic nitrogen-containing compound used can be varied within wide limits. Usually the amount of organic nitrogen-containing compound added corresponds to a mole ratio of Si:N of from 2:1 to 100:1, suitably from 3:1 to 60:1 and preferably from 4:1 to 40:1.
  • step (d) of the process when using an aqueous alkali metal silicate to adjust the pH of the aqueous phase, the weight ratio of alkali metal silicate used is step (b) to alkali metal silicate used is step (d) can vary within wide limits; usually the ratio is in the range 99:1 to 1:9, suitably from 19:1 to 1:2, preferably from 4:1 to 1:1.
  • step (e) of the process the ion exchange resin is separated from the aqueous phase, for example by filtration. This can be done after step (c), for example after step (c) but before step (d), or after step (d). It is also possible to separate the ion exchange resin from the aqueous phase during step (d). For example, the ion exchange resin can be separated after adding an alkaline material but before adding a second material. It is also possible to add part of one alkaline material, e.g. aqueous alkali metal silicate, then separating the ion exchange resin from the aqueous phase followed by adding the remaining part of the alkaline material. Preferably, the ion exchange resin is separated from the aqueous phase after step (d).
  • the concentration of the aqueous starting materials used in the process is preferably adjusted so as to provide a silica-based sol which usually has a SiO 2 content of at least 3% by weight, suitably at least 5%, preferably at least 6%, most preferably at least 7.5%, and suitably up to 20% by weight, preferably up to 15% by weight.
  • the aqueous silica-based sol according to the invention contains silica-based particles, i.e. particles based on silica or SiO 2 , that are preferably anionic and colloidal, i.e., in the colloidal range of particle size.
  • the particles can be and are suitably modified with aluminium, preferably surface modified with aluminium.
  • the silica-based sol of the invention can have a mole ratio of Si:Al of from 10:1 to 100:1, suitably from 20:1 to 50:1, preferably from 25:1 to 35:1, and most preferably from 25:1 to 30:1.
  • the silica-based sol according to the invention can be modified with an organic nitrogen-containing compound.
  • the silica-based sol of the invention can have a mole ratio of Si:N of from 2:1 to 100:1, suitably from 3:1 to 60:1 and preferably from 4:1 to 40:1.
  • the silica-based sol of the invention can have an S value in the range of from 10 to 50%, suitably from to 12 to 40%, preferably from 15 to 25%, and most preferably from 17 to 24%.
  • the S-value is measured and calculated as described by Iler & Dalton in J. Phys. Chem. 60 (1956), 955-957.
  • the S-value indicates the degree of aggregate or microgel formation and a lower S-value is indicative of a higher degree of aggregation.
  • the silica-based particles present in the sol can have a specific surface area of at least 300 m 2 /g, suitably at least 700 m 2 /g, preferably at least 750 m 2 /g.
  • the specific surface area is usually up to 1,000 m 2 /g, suitably up to 950 m 2 /g.
  • the specific surface area is measured by means of titration with NaOH as described by Sears in Analytical Chemistry 28 (1956):12, 1981-1983, after appropriate removal of or adjustment for any compounds present in the sample that may disturb the titration like aluminium, nitrogen and boron compounds, for example as described by Sears and in U.S. Pat. No. 5,176,891.
  • the silica-based sol of this invention is preferably stable.
  • the sol maintains a specific surface area of at least 300 m 2 /g, preferably at least 700 m 2 /g, for at least 3 months on storage or ageing at 20° C. in dark and non-agitated conditions.
  • the sol maintains an S value in the range of from 10 to 50%, preferably from 12 to 40%, for at least 3 months on storage or ageing at 20° C. in dark and non-agitated conditions.
  • the silica-based sol according to this invention is suitable for use as a flocculating agent, for example in the production of pulp and paper, notably as a drainage and retention aid, and within the field of water purification, both for purification of different kinds of waste water and for purification specifically of white water from the pulp and paper industry.
  • the silica-based sols can be used as a flocculating agent, notably as a drainage and retention aid, in combination with organic polymers which can be selected from anionic, amphoteric, non-ionic and cationic polymers and mixtures thereof.
  • organic polymers which can be selected from anionic, amphoteric, non-ionic and cationic polymers and mixtures thereof.
  • the use of such polymers as flocculating agents and as drainage and retention aids is well known in the art.
  • the polymers can be derived from natural or synthetic sources, and they can be linear, branched or cross-linked.
  • generally suitable main polymers include anionic, amphoteric and cationic starches; anionic, amphoteric and cationic acrylamide-based polymers, including essentially linear, branched and cross-linked anionic and cationic acrylamide-based polymers; as well as cationic poly(diallyldimethyl ammonium chloride); cationic polyethylene imines; cationic polyamines; cationic polyamideamines and vinylamide-based polymers, melamine-formaldehyde and urea-formaldehyde resins.
  • the silica-based sols are used in combination with at least one cationic or amphoteric polymer, preferably cationic polymer.
  • Cationic starch and cationic polyacrylamide are particularly preferred polymers and they can be used singly, together with each other or together with other polymers, e.g. other cationic and/or anionic polymers.
  • the molecular weight of the polymer is suitably above 1,000,000 and preferably above 2,000,000. The upper limit is not critical; it can be about 50,000,000, usually 30,000,000 and suitably about 25,000,000. However, the molecular weight of polymers derived from natural sources may be higher.
  • the present silica-based sol can also be used in combination with cationic coagulant(s), either with or without the co-use of the organic polymer(s) described above.
  • suitable cationic coagulants include water-soluble organic polymeric coagulants and inorganic coagulants.
  • the cationic coagulants can be used singly or together, i.e. a polymeric coagulant can be used in combination with an inorganic coagulant.
  • suitable water-soluble organic polymeric cationic coagulants include cationic polyamines, polyamideamines, polyethylene imines, dicyandiamide condensation polymers and polymers of water soluble ethylenically unsaturated monomer or monomer blend which is formed of 50 to 100 mole % cationic monomer and 0 to 50 mole % other monomer.
  • the amount of cationic monomer is usually at least 80 mole %, suitably 100%.
  • suitable ethylenically unsaturated cationic monomers include dialkylaminoalkyl (meth)-acrylates and -acrylamides, preferably in quaternised form, and diallyl dialkyl ammonium chlorides, e.g.
  • diallyl dimethyl ammonium chloride preferably homopolymers and copolymers of DADMAC.
  • the organic polymeric cationic coagulants usually have a molecular weight in the range of from 1,000 to 700,000, suitably from 10,000 to 500,000.
  • suitable inorganic coagulants include aluminium compounds, e.g. alum and polyaluminium compounds, e.g. polyaluminium chlorides, polyaluminium sulphates, polyaluminium silicate sulphates and mixtures thereof.
  • the components of the drainage and retention aids according to the invention can be added to the stock in conventional manner and in any order.
  • drainage and retention aids comprising a silica-based sol and organic polymer
  • a cationic coagulant it is preferably added to the cellulosic suspension before the addition of the silica-based sol, preferably also before the addition of the organic polymer(s).
  • the components of the drainage and retention aids according to the invention are added to the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type and number of components, type of furnish, filler content, type of filler, point of addition, etc. Generally the components are added in amounts that give better drainage and retention than is obtained when not adding the components.
  • the silica-based sol is usually added in an amount of at least 0.001% by weight, often at least 0.005% by weight, calculated as SiO 2 and based on dry furnish, i.e. dry cellulosic fibres and optional fillers, and the upper limit is usually 1.0% and suitably 0.5% by weight.
  • the organic polymer is usually added in an amount of at least 0.001%, often at least 0.005% by weight, based on dry furnish, and the upper limit is usually 3% and suitably 1.5% by weight.
  • a cationic polymeric coagulant it can be added in an amount of at least 0.05%, based on dry furnish.
  • the amount is in the range of from 0.07 to 0.5%, preferably in the range from 0.1 to 0.35%.
  • the total amount added is usually at least 0.05%, calculated as Al 2 O 3 and based on dry furnish.
  • the amount is in the range of from 0.1 to 3.0%, preferably in the range from 0.5 to 2.0%.
  • additives which are conventional in papermaking can of course be used in combination with the additives according to the invention, such as, for example, dry strength agents, wet strength agents, optical brightening agents, dyes, sizing agents like rosin-based sizing agents and cellulose-reactive sizing agents, e.g. alkyl and alkenyl ketene dimers and ketene multimers, alkyl and alkenyl succinic anhydrides, etc.
  • the cellulosic suspension, or stock can also contain mineral fillers of conventional types such as, for example, kaolin, china clay, titanium dioxide, gypsum, talc and natural and synthetic calcium carbonates such as chalk, ground marble and precipitated calcium carbonate.
  • the process of this invention is used for the production of paper.
  • paper as used herein, of course include not only paper and the production thereof, but also other cellulosic sheet or web-like products, such as for example board and paperboard, and the production thereof.
  • the process can be used in the production of paper from different types of suspensions of cellulose-containing fibres and the suspensions should suitably contain at least 25% by weight and preferably at least 50% by weight of such fibres, based on dry substance.
  • the suspension can be based on fibres from chemical pulp such as sulphate, sulphite and organosolv pulps, mechanical pulp such as thermomechanical pulp, chemothermomechanical pulp, refiner pulp and groundwood pulp, from both hardwood and softwood, and can also be based on recycled fibres, optionally from de-inked pulps, and mixtures thereof.
  • the pH of the suspension, the stock can be within the range of from about 3 to about 10.
  • the pH is suitably above 3.5 and preferably within the range of from 4 to 9.
  • This example illustrates the preparation of a silica-based sol according to the invention: Regenerated ion exchange resin (471 g) and water (1,252 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (298 g) was then added to the slurry at a rate of 5 g/min. After the addition of sodium silicate, the pH of the slurry was about 7.3. The slurry was then stirred for another 44 minutes, whereupon the pH of the aqueous phase was 6.9. Thereafter additional aqueous sodium silicate (487 g) was added to the slurry at a rate of 5 g/min. The obtained silica-based sol was separated from the ion exchange resin.
  • This example illustrates the preparation of another silica-based sol according to the invention: Aqueous sodium aluminate (52 g) was added to the sol (527.4 g) according to Example 1 under vigorous stirring during a period of 10 min.
  • This example illustrates the preparation of yet another silica-based sol according to the invention: Aqueous choline hydroxide (7.9 g) was added to the sol (395 g) according to Example 1 under vigorous stirring at a rate of 4 g/min.
  • This example illustrates the preparation of still another silica-based sol according to the invention: Regenerated ion exchange resin (600 g) and water (1,600 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (764 g) was then added to the slurry at a rate of 6.8 g/min. After the addition of sodium silicate, the pH of the slurry was about 8, whereupon the ion exchange resin was separated from the aqueous phase. Aqueous sodium hydroxide (30 g) was added to the aqueous phase at the rate of 10 g/min.
  • This example illustrates the preparation of another silica-based sol according to the invention: Aqueous sodium aluminate (83 g) was added to the sol (776 g) according to Example 4 under vigorous stirring during a period of 10 min.
  • This example illustrates the preparation of yet another silica-based sol according to the invention: Aqueous choline hydroxide (14.3 g) was added to the sol (714 g) according to Example 4 under vigorous stirring at a rate of 4 g/min.
  • This example illustrates the preparation of yet another silica-based sol according to the invention: Regenerated ion exchange resin (595 g) and water (1,605 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (849 g) was then added to the slurry at a rate of 6.3 g/min. The slurry was then stirred for another 135 minutes, whereupon the pH of the aqueous phase was 7.9. Thereafter additional aqueous sodium silicate (326 g) was added to the slurry at a rate of 6.3 g/min. The obtained silica-based sol was separated from the ion exchange resin.
  • silica-based sols Ref. 1a to Ref. 3, were prepared for comparison purposes:
  • Ref. 1a is a silica-based sol prepared according to the disclosure of Example 4 of U.S. Pat. Nos. 6,372,089 and 6,372,806.
  • Ref. 1b is a silica-based sol prepared according to the general disclosure of column 4 of U.S. Pat. Nos. 6,372,089 and 6,372,806, wherein in step (c) the contents of the reaction vessel was stirred until the pH of the contents of the vessel was 9.2
  • Ref. 1c is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,447,604 which had an S-value of about 25%, a mole ratio of Si:Al of about 19 and contained silica particles with a specific surface area of about 900 m 2 /g SiO 2 .
  • Ref. 1d is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,603,805 with an S-value of 34% and contained silica particles with a specific surface area of about 700 m 2 /g.
  • Ref. 2a is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,368,833 which had an S-value of about 25%, a mole ratio of Si:Al of about 19 and contained silica particles with a specific surface area of about 900 m 2 /g SiO 2 which were surface-modified with aluminium.
  • Ref. 2b is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,368,833 which had an S-value of 20%, a mole ratio of Si:Al of about 18 and contained silica particles with a specific surface area of about 820 m 2 /g SiO 2 which were surface-modified with aluminium.
  • Ref. 3 is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 6,379,500 which had an S-value of about 30%, mole ratio of Si:Na of about 10, mole ratio of Si:N of about 21, and contained choline hydroxide and silica particles with a specific surface area of about 900 m 2 /g SiO 2 .
  • the stock used was based on a standard fine paper furnish consisting of 60° A bleached birch sulfate and 40% bleached pine sulfate. 30% ground calcium carbonate was added to the stock as filler and 0.3 g/l of Na 2 SO 4 .10H 2 O was added to increase conductivity. Stock pH was 8.1, conductivity 1.5 mS/cm and consistency 0.5%.
  • the silica-based sols were tested in conjunction with a cationic polymer being cationic starch having a degree of substitution of about 0.042. The starch was added in an amount of 8 kg/tonne, calculated as dry starch on dry furnish.
  • the stock was stirred in a baffled jar at a speed of 1,500 rpm throughout the test and chemical additions to the stock were made as follows:
  • Tables 1 to 3 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO 2 and based on dry furnish.
  • silica-based sols according to Examples 1 to 3 were further evaluated following the procedure of Example 9 except that a cationic polyacrylamide (“PAM”) was used instead of cationic starch.
  • PAM cationic polyacrylamide
  • the stock was stirred in a baffled jar at a speed of 1,500 rpm throughout the test and chemical additions to the stock were made as follows:
  • Tables 4 to 6 show the results obtained when using different dosages of cationic polyacrylamide, kg/tonne, calculated as dry starch on dry furnish, and silica-based sol, kg/tonne, calculated as SiO 2 and based on dry furnish.
  • silica-based sols according to Examples 4 to 6 were tested against silica-based sols according to Example 8 following the procedure of Example 9.
  • Tables 7 to 9 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO 2 and based on dry furnish.
  • silica-based sols according to Examples 4 to 6 were tested against silica-based sols according to Example 8 following the procedure of Example 10.
  • Tables 10 to 12 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO 2 and based on dry furnish.
  • Example 7 The silica-based sol according to Example 7 was tested against a silica-based sol according to Example 8 following the procedure of Example 9.
  • Table 13 shows the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO 2 and based on dry furnish.

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Abstract

The invention relates to a process for producing aqueous silica-based sols which comprises providing a cationic ion exchange resin having at least part of its ion exchange capacity in hydrogen form; bringing said ion exchange resin in contact with an aqueous alkali metal silicate to form an aqueous slurry; adjusting the pH of the aqueous slurry and separating the ion exchange resin from the aqueous slurry, as well as the silica-based sols obtained by the process; the invention also relates to silica-based sols obtained by the process, as well as a process for producing paper which comprises providing an aqueous suspension comprising cellulosic fibres; adding to the suspension one or more drainage and retention aids comprising a silica-based sol according to the invention; and dewatering the obtained suspension to provide a sheet or web of paper.

Description

This application is a Continuation application of U.S. patent application Ser. No. 11/100,929 filed Apr. 7, 2005, now U.S. Pat. No. 7,732,495, which claims priority based on U.S. Provisional Patent Application No. 60/559,958, filed Apr. 7, 2004 and Ser. No. 60/559,965, filed Apr. 7, 2004.
FIELD OF THE INVENTION
The present invention generally relates to silica-based sols suitable for use in papermaking. More particularly, the invention relates to silica-based sols, their production and use in papermaking. The present invention provides an improved method of producing silica-based sols with high stability and SiO2 contents as well as improved drainage performance.
BACKGROUND OF THE INVENTION
In the papermaking art, an aqueous suspension containing cellulosic fibres and optional fillers and additives, referred to as stock, is fed into a headbox which ejects the stock onto a forming wire. Water is drained from the stock so that a wet web of paper is formed on the wire, and the web is further dewatered and dried in the drying section of the paper machine. Drainage and retention aids are conventionally introduced into the stock in order to facilitate drainage and to increase adsorption of fine particles onto the cellulosic fibres so that they are retained with the fibres on the wire.
Sols of silica-based particles are widely used as drainage and retention aids in combination with charged organic polymers. Such additive systems are among the most efficient now in use in the papermaking industry. One of the parameters affecting the properties and performance of silica-based sols is the specific surface area; stable, high-performance silica-based sols usually contain particles with a specific surface area of at least 300 m2/g. Another parameter is the S value, which indicates the degree of aggregate or microgel formation; a lower S-value is indicative of a higher degree of aggregation. While high surface areas and a certain degree of aggregate or microgel formation may be advantageous from a performance point of view, very high surface areas and extensive particle aggregation or microgel formation result in considerably decreased stability of silica-based sols, thereby making extreme dilution of the sols necessary so as to avoid gel formation.
U.S. Pat. No. 5,368,833 discloses a silica sol comprising silica particles having a specific surface area within the range of from 750 to 1,000 m2/g which are surface-modified with aluminium to a degree of from 2 to 25% substitution of silicon atoms, and wherein the sol has an S value within the range of from 8 to 45%. Said patent also discloses a process for producing the silica sol which comprises the steps of acidifying a water glass solution to a pH within the range of from 1 to 4; alkalising the acid sol at an SiO2 content within the range of from 7 to 4.5% by weight; allowing particle growth of the sol to a specific surface area within the range of from 750 to 1,000 m2/g; and subjecting the sol to aluminium modification.
U.S. Pat. No. 5,603,805 discloses silica sols having an S value within the range of from 15 to 40% comprising anionic silica particles, said silica particles optionally being aluminium modified, and having a specific surface area within the range of from 300 to 700 m2/g. Said patent also discloses a process for producing the silica sol comprising the steps of acidifying a water glass solution to a pH within the range of from 1 to 4; alkalising the acid sol at an SiO2 content within the range of from 7 to 5% by weight; alternatively alkalisation of the acid sol to a pH value between 7 and 9; and particle growth of the sol to a specific surface area within the range of from 300 to 700 m2/g; and optionally followed by aluminium modification.
International Patent Appln. Publ. No. WO 98/56715 discloses a process for preparing an aqueous polysilicate microgel which comprises mixing an aqueous solution of an alkali metal silicate with an aqueous phase of a silica-based material having a pH of 11 or less. The polysilicate microgel is used as a flocculating agent in combination with at least one cationic or amphoteric polymer in the production of pulp and paper and for water purification.
International Patent Appln. Publ. No. WO 00/66492 discloses a process for the production of an aqueous sol containing silica-based particles which comprises acidifying an aqueous silicate solution to a pH of from 1 to 4 to form an acid sol; alkalising the acid sol in a first alkalisation step; allowing particle growth of the alkalised sol for at least 10 minutes and/or heat-treating the alkalised sol at a temperature of at least 30° C.; alkalising the obtained sol in a second alkalisation step; and optionally modifying the silica-based sol with, for example, aluminium.
U.S. Pat. No. 6,372,806 discloses a process for preparing a stable colloidal silica having an S-value of from 20-50 and wherein said silica has a surface area of greater than 700 m2/g comprising: (a) charging a reaction vessel with a cationic ion exchange resin having at least 40 percent of its ion exchange capacity in the hydrogen form wherein said reaction vessel has means for separating said colloidal silica from said ion exchange resin; (b) charging said reaction vessel with an aqueous alkali metal silicate having a mole ratio of SiO2 to alkali metal oxide in the range of from 15:1 to 1:1 and a pH of at least 10.0; (c) stirring the contents of said reaction vessel until the pH of said contents is in the range of from 8.5 to 11.0; (d) adjusting the pH of the contents of said reaction vessel to above 10.0 using an additional amount of said alkali metal silicate; and (e) separating the resulting colloidal silica from said ion exchange resin while removing said colloidal silica from said reaction vessel.
U.S. Pat. No. 5,176,891 discloses a method for the production of water soluble polyaluminosilicate microgels having a surface area of at least about 1,000 m2/g, comprising the steps of (a) acidifying a dilute solution of alkali metal silicate containing about 0.1 to 6 wt. % SiO2 to a pH of between 2 and 10.5 to produce polysilicic acid; followed by (b) reacting a water soluble aluminate with the polysilicic acid before the polysilicic acid has gelled such that a product with an alumina/silica mole ratio greater than about 1/100 is obtained; and then (c) diluting the reaction mix before gelation has occurred to the equivalence of about 2.0 wt. % SiO2 or less to stabilize the microgels.
It would be advantageous to be able to provide silica-based sols with high stability and SiO2 contents as well as improved drainage performance. It would also be advantageous to be able to provide improved processes for the preparation of silica-based sols with stability and SiO2 contents as well as improved drainage performance. It would also be advantageous to be able to provide a papermaking process with improved drainage.
SUMMARY OF THE INVENTION
The present invention is generally directed to a process for producing a silica-based sol which comprises:
    • (a) providing a cationic ion exchange resin having at least part of its ion exchange capacity in hydrogen form;
    • (b) bringing said ion exchange resin in contact with an aqueous alkali metal silicate to form an aqueous slurry;
    • (c) stirring said aqueous slurry until the pH of the aqueous phase is in the range of from 5.0 to 8.0;
    • (d) adjusting the pH of said aqueous phase to above 9.0; and
    • (e) separating said ion exchange resin from the aqueous phase after step (c) or after step (d), and optionally
    • (f) obtaining an aqueous silica-based sol having an S value between 10 and 50%.
The invention is further generally directed to a process for producing a silica-based sol which comprises:
    • (a) providing a reaction vessel;
    • (b) providing in said reaction vessel:
      • (i) a cationic ion exchange resin having at least part of its ion exchange capacity in hydrogen form, and
      • (ii) an aqueous alkali metal silicate,
      • to form an aqueous slurry;
    • (c) stirring said aqueous slurry until the pH of the aqueous phase is in the range of from 5.0 to 8.0;
    • (d) adding one or more materials to the aqueous phase obtained after step (c) to form an aqueous phase having a pH of above 9.0;
    • (e) separating said ion exchange resin from the aqueous phase after step (c) or after step (d); and, optionally,
    • (f) obtaining an aqueous silica-based sol having an S value between 10 and 50%.
The invention is further directed to a silica-based sol and a silica-based sol obtainable by the processes. The invention is further directed to uses of the silica-based sol according to the invention, in particular as a drainage and retention aid in papermaking and for water purification.
The invention is further generally directed to a process for producing paper which comprises
    • (a) providing an aqueous suspension comprising cellulosic fibres;
    • (b) adding to the suspension one or more drainage and retention aids comprising a silica-based sol according to the invention as defined herein; and
    • (c) dewatering the obtained suspension to provide a sheet or web of paper.
DETAILED DESCRIPTION OF THE INVENTION
In accordance with the present invention there is provided silica-based sols which are suitable for use as flocculating agents in water purification and as drainage and retention aids in papermaking. The silica-based sols of the invention exhibit good stability over extended periods of time, notably high surface area stability and high stability to avoid complete gel formation. The silica-based sols further result in very good drainage and retention when used in papermaking, in particular improved drainage. Hereby the present invention makes it possible to increase the speed of the paper machine and to use a lower dosage of additive to give a corresponding drainage effect, thereby leading to an improved papermaking process and economic benefits. The silica-based sols of the invention can be prepared by a process that is simple, quick and easy to control and regulate, and the process makes it possible to utilize simple and less expensive production equipment. Hereby the silica-sols of the invention can be produced by a process that is simplified, improved and more economic.
The ion exchange resin used in the process is cationic and has at least part of its ion exchange capacity in the hydrogen form, i.e. an acid cationic ion exchange resin, preferably a weak acid cationic ion exchange resin. Suitably, the ion exchange resin has at least 40% of its ion exchange capacity in the hydrogen form, preferably at least 50%. Suitable ion exchange resins are provided on the market by several manufacturers, for example Amberlite® IRC84SP from Rohm & Haas. Preferably, a reaction vessel equipped with means for mixing, e.g. a stirrer, is charged with the ion exchange resin. Preferably, the ion exchange resin is regenerated by addition of an acid, e.g. sulphuric acid, preferably according to manufacturer's instruction.
Step (b) of the process comprises bringing together the cationic ion exchange resin with an aqueous alkali metal silicate. Suitably, this is achieved by adding the ion exchange resin and aqueous alkali metal silicate to the reaction vessel. Preferably, a reaction vessel containing regenerated ion exchange resin is charged with the aqueous alkali metal silicate whereby an aqueous slurry is formed. Usually, the aqueous alkali metal silicate is added to a reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form at a rate in the range of from 0.5 to 50 g SiO2 per minute and kg ion exchange resin, calculated as ion exchange resin having 100% of its ion exchange capacity in hydrogen form, suitably from 1 to 35, and preferably from 2 to 20. Alternatively, a reaction vessel containing the aqueous alkali metal silicate is charged with the regenerated ion exchange resin whereby an aqueous slurry is formed.
Examples of suitable aqueous alkali metal silicates or water glass include conventional materials, e.g. lithium, sodium and potassium silicates, preferably sodium silicate. The molar ratio of silica to alkali metal oxide, e.g. SiO2 to Na2O, K2O or Li2O, or a mixture thereof, in the silicate solution can be in the range of from 15:1 to 1:1, suitably in the range of from 4.5:1 to 1.5:1, preferably from 3.9:1 to 2.5:1. The aqueous alkali metal silicate used can have an SiO2 content of from about 2 to about 35% by weight, suitably from about 5 to about 30% by weight, and preferably from about 15 to about 25% by weight. The pH of the aqueous alkali metal silicate is usually above 11, typically above 12.
Step (c) of the process comprises stirring the aqueous slurry formed in step (b) until the pH of the aqueous phase is in the range of from 5.0 to 8.0. Suitably stirring is carried out until the pH of the aqueous phase is in the range of from 6.0 to 8.0, preferably from 6.5 to 7.5. Preferably, particle growth takes place while stirring the aqueous slurry. The silica-based particles formed usually have a specific surface area of at least 300 m2/g, preferably at least 700 m2/g. The specific surface area is suitably up to 1,500 m2/g, preferably up to 1,000 m2/g. Preferably, the slurry is stirred to allow particle aggregation and microgel formation, usually corresponding to an S value in the range of from 5 to 45%, suitably from 8 to 35%, preferably from 10 to 25% and most preferably from 15 to 23%. The stirring usually takes place during a period of time of from 5 to 240 minutes, preferably from 15 to 120 minutes.
Step (c) of the process can be carried out simultaneously with and/or after step (b). In a preferred embodiment, the aqueous alkali metal silicate is added under stirring to the reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form and then, after completed addition, the stirring continues to achieve the pH and optionally particle aggregation or microgel formation as described above. In another preferred embodiment, the aqueous alkali metal silicate is added under stirring to the reaction vessel containing ion exchange resin having at least part of its ion exchange capacity in hydrogen form to achieve the pH and optionally particle aggregation or microgel formation as described above.
Step (d) of the process comprises adding to the aqueous phase one or more materials. Hereby the pH of the aqueous phase is suitably adjusted to above 9.0, preferably raised to a pH above 10.0; suitably the pH is in the range of from 9.2 to 11.5, preferably from 9.5 to 11.2, and most preferably from 10.0 to 11.0. Preferably, at least one alkaline material is added, either singly or in combination with at least one second material.
Examples of suitable alkaline materials include aqueous alkali metal silicates, e.g. any of those defined above, preferably sodium silicate; aqueous alkali metal hydroxides, e.g. sodium and potassium hydroxides, preferably sodium hydroxide; ammonium hydroxide; alkaline aluminium salts, e.g. aluminates, suitably aqueous aluminates, e.g. sodium and potassium aluminates, preferably sodium aluminate.
Examples of suitable second materials include aluminium compounds and organic nitrogen-containing compounds. Examples of suitable aluminium compounds include neutral and essentially neutral aluminium salts, e.g. aluminium nitrate, alkaline aluminium salts, e.g. any of those defined above, preferably sodium aluminate.
Examples of suitable organic nitrogen-containing compounds include primary amines, secondary amines, tertiary amines and quaternary amines, the latter also referred to as quaternary ammonium compounds. The nitrogen-containing compound is preferably water-soluble or water-dispersible. The amine can be uncharged or cationic. Examples of cationic amines include acid addition salts of primary, secondary and tertiary amines and, preferably, quaternary ammonium compounds, as well as their hydroxides. The organic nitrogen-containing compound usually has a molecular weight below 1,000, suitably below 500 and preferably below 300. Preferably, a low molecular weight organic nitrogen-containing compound is used, for example those compounds having up to 25 carbon atoms, suitably up to 20 carbon atoms, preferably from 2 to 12 carbon atoms and most preferably from 2 to 8 carbon atoms. In a preferred embodiment, the organic nitrogen-containing compound has one or more oxygen-containing substituents, for example with oxygen in the form of hydroxyl groups and/or alkyloxy groups. Examples of preferred substituents of this type include hydroxy alkyl groups, e.g. ethanol groups, and methoxy and ethoxy groups. The organic nitrogen-containing compounds may include one or more nitrogen atoms, preferably one or two. Preferred amines include those having a pKa value of at least 6, suitably at least 7 and preferably at least 7.5.
Examples of suitable primary amines, i.e. amines having one organic substituent, include alkyl amines, e.g. propyl amine, butyl amine and cyclohexyl amine; alkanol amines, e.g. ethanol amine; and alkoxyalkyl amines, e.g. 2-methoxyethyl amine. Examples of suitable secondary amines, i.e. amines having two organic substituents, include dialkyl amines, e.g. diethyl amine, dipropyl amine and di-isopropyl amine; dialkanol amines, e.g. diethanol amine, and pyrrolidine. Examples of suitable tertiary amines, i.e. amines having three organic substituents, include trialkyl amines, e.g. triethyl amine; trialkanol amines, e.g. triethanol amine; N,N-dialkyl alkanol amines, e.g. N,N-dimethyl ethanol amine. Examples of suitable quaternary amines, or quaternary ammonium compounds, i.e. amines having four organic substituents, include tetraalkanol amines, e.g. tetraethanol ammonium hydroxide and tetraethanol ammonium chloride; quaternary amines or ammonium compounds with both alkanol and alkyl substituents such as N-alkyltrialkanol amines, e.g. methyltriethanol ammonium hydroxide and methyltriethanol ammonium chloride; N,N-dialkyldialkanol amines, e.g. dimethyl diethanol ammonium hydroxide and dimethyl diethanol ammonium chloride; N,N,N-trialkyl alkanol amines, e.g. choline hydroxide and choline chloride; N,N,N-trialkyl benzyl amines, e.g. dimethyl cocobenzyl ammonium hydroxide, dimethyl cocobenzyl ammonium chloride and trimethyl benzyl ammonium hydroxide; tetraalkyl ammonium salts, e.g. tetramethyl ammonium hydroxide, tetramethyl ammonium chloride, tetraethyl ammonium hydroxide, tetraethyl ammonium chloride, tetra-propyl ammonium hydroxide, tetrapropyl ammonium chloride, diethyldimethyl ammonium hydroxide, diethyldimethyl ammonium chloride, triethylmethyl ammonium hydroxide and triethylmethyl ammonium chloride. Examples of suitable diamines include aminoalkylalkanol amines, e.g. aminoethylethanol amine, piperazine and nitrogen-substituted piperazines having one or two lower alkyl groups of 1 to 4 carbon atoms. Examples of preferred organic nitrogen-containing compounds include triethanol amine, diethanol-amine, dipropyl amine, aminoethyl ethanol amine, 2-methoxyethyl amine, N,N-dimethyl-ethanol amine, choline hydroxide, choline chloride, tetramethyl ammonium hydroxide, tetraethyl ammonium hydroxide and tetraethanol ammonium hydroxide.
Preferably, aqueous alkali metal silicate is added, either singly or in combination with aqueous sodium aluminate or aqueous organic nitrogen-containing compound.
When using two or more materials comprising at least one alkaline material and at least one second material, the materials can be added in any order, preferably the alkaline material is added first followed by adding the second material.
In a preferred embodiment, alkali metal silicate, e.g. sodium silicate, is added first and then an alkaline aluminium salt, e.g. aqueous sodium aluminate, is added. In another preferred embodiment, aqueous alkali metal hydroxide, e.g. sodium hydroxide, is added first and then an alkaline aluminium salt, e.g. aqueous sodium aluminate, is added. The addition of aluminium compound provides an aluminated silica-based sol. Suitably, the addition of aluminium compound results in aluminium modification of the silica-based particles, preferably the particles are surface-modified by aluminium. The amount of aluminium compound used can be varied within wide limits. Usually the amount of aluminium compound added corresponds to a mole ratio of Si:Al of from 10:1 to 100:1, suitably from 20:1 to 50:1, preferably from 25:1 to 35:1, and most preferably from 25:1 to 30:1.
In another preferred embodiment, alkali metal silicate, e.g. sodium silicate, is added first and then an organic nitrogen-containing compound, e.g. aqueous choline hydroxide, is added. In another preferred embodiment, aqueous alkali metal hydroxide, e.g. sodium hydroxide, is added first and then an organic nitrogen-containing compound, e.g. aqueous choline hydroxide, is added. The addition of organic nitrogen-containing compound provides a nitrogen-modified silica-based sol. The amount of organic nitrogen-containing compound used can be varied within wide limits. Usually the amount of organic nitrogen-containing compound added corresponds to a mole ratio of Si:N of from 2:1 to 100:1, suitably from 3:1 to 60:1 and preferably from 4:1 to 40:1.
In step (d) of the process, when using an aqueous alkali metal silicate to adjust the pH of the aqueous phase, the weight ratio of alkali metal silicate used is step (b) to alkali metal silicate used is step (d) can vary within wide limits; usually the ratio is in the range 99:1 to 1:9, suitably from 19:1 to 1:2, preferably from 4:1 to 1:1.
In step (e) of the process, the ion exchange resin is separated from the aqueous phase, for example by filtration. This can be done after step (c), for example after step (c) but before step (d), or after step (d). It is also possible to separate the ion exchange resin from the aqueous phase during step (d). For example, the ion exchange resin can be separated after adding an alkaline material but before adding a second material. It is also possible to add part of one alkaline material, e.g. aqueous alkali metal silicate, then separating the ion exchange resin from the aqueous phase followed by adding the remaining part of the alkaline material. Preferably, the ion exchange resin is separated from the aqueous phase after step (d).
The concentration of the aqueous starting materials used in the process, e.g. the aqueous alkali metal silicate, aqueous alkali metal hydroxide and aqueous sodium aluminate, is preferably adjusted so as to provide a silica-based sol which usually has a SiO2 content of at least 3% by weight, suitably at least 5%, preferably at least 6%, most preferably at least 7.5%, and suitably up to 20% by weight, preferably up to 15% by weight.
The aqueous silica-based sol according to the invention contains silica-based particles, i.e. particles based on silica or SiO2, that are preferably anionic and colloidal, i.e., in the colloidal range of particle size. The particles can be and are suitably modified with aluminium, preferably surface modified with aluminium. The silica-based sol of the invention can have a mole ratio of Si:Al of from 10:1 to 100:1, suitably from 20:1 to 50:1, preferably from 25:1 to 35:1, and most preferably from 25:1 to 30:1.
The silica-based sol according to the invention can be modified with an organic nitrogen-containing compound. The silica-based sol of the invention can have a mole ratio of Si:N of from 2:1 to 100:1, suitably from 3:1 to 60:1 and preferably from 4:1 to 40:1.
The silica-based sol of the invention can have an S value in the range of from 10 to 50%, suitably from to 12 to 40%, preferably from 15 to 25%, and most preferably from 17 to 24%. The S-value is measured and calculated as described by Iler & Dalton in J. Phys. Chem. 60 (1956), 955-957. The S-value indicates the degree of aggregate or microgel formation and a lower S-value is indicative of a higher degree of aggregation.
The silica-based particles present in the sol can have a specific surface area of at least 300 m2/g, suitably at least 700 m2/g, preferably at least 750 m2/g. The specific surface area is usually up to 1,000 m2/g, suitably up to 950 m2/g. The specific surface area is measured by means of titration with NaOH as described by Sears in Analytical Chemistry 28 (1956):12, 1981-1983, after appropriate removal of or adjustment for any compounds present in the sample that may disturb the titration like aluminium, nitrogen and boron compounds, for example as described by Sears and in U.S. Pat. No. 5,176,891.
The silica-based sol of the invention usually has a mole ratio of Si:X, where X=alkali metal, of at least 3:1, suitably at least 4:1, preferably at least 5:1 and most preferably at least 6:1. The mole ratio of Si:X, where X=alkali metal, is usually up to 50:1, suitably up to 20:1, preferably up to 17:1, more preferably up to 15:1 and most preferably up to 10:1.
The silica-based sol of this invention is preferably stable. Suitably, the sol maintains a specific surface area of at least 300 m2/g, preferably at least 700 m2/g, for at least 3 months on storage or ageing at 20° C. in dark and non-agitated conditions. Suitably, the sol maintains an S value in the range of from 10 to 50%, preferably from 12 to 40%, for at least 3 months on storage or ageing at 20° C. in dark and non-agitated conditions.
The silica-based sol according to this invention is suitable for use as a flocculating agent, for example in the production of pulp and paper, notably as a drainage and retention aid, and within the field of water purification, both for purification of different kinds of waste water and for purification specifically of white water from the pulp and paper industry. The silica-based sols can be used as a flocculating agent, notably as a drainage and retention aid, in combination with organic polymers which can be selected from anionic, amphoteric, non-ionic and cationic polymers and mixtures thereof. The use of such polymers as flocculating agents and as drainage and retention aids is well known in the art. The polymers can be derived from natural or synthetic sources, and they can be linear, branched or cross-linked. Examples of generally suitable main polymers include anionic, amphoteric and cationic starches; anionic, amphoteric and cationic acrylamide-based polymers, including essentially linear, branched and cross-linked anionic and cationic acrylamide-based polymers; as well as cationic poly(diallyldimethyl ammonium chloride); cationic polyethylene imines; cationic polyamines; cationic polyamideamines and vinylamide-based polymers, melamine-formaldehyde and urea-formaldehyde resins. Suitably, the silica-based sols are used in combination with at least one cationic or amphoteric polymer, preferably cationic polymer. Cationic starch and cationic polyacrylamide are particularly preferred polymers and they can be used singly, together with each other or together with other polymers, e.g. other cationic and/or anionic polymers. The molecular weight of the polymer is suitably above 1,000,000 and preferably above 2,000,000. The upper limit is not critical; it can be about 50,000,000, usually 30,000,000 and suitably about 25,000,000. However, the molecular weight of polymers derived from natural sources may be higher.
The present silica-based sol can also be used in combination with cationic coagulant(s), either with or without the co-use of the organic polymer(s) described above. Examples of suitable cationic coagulants include water-soluble organic polymeric coagulants and inorganic coagulants. The cationic coagulants can be used singly or together, i.e. a polymeric coagulant can be used in combination with an inorganic coagulant.
Examples of suitable water-soluble organic polymeric cationic coagulants include cationic polyamines, polyamideamines, polyethylene imines, dicyandiamide condensation polymers and polymers of water soluble ethylenically unsaturated monomer or monomer blend which is formed of 50 to 100 mole % cationic monomer and 0 to 50 mole % other monomer. The amount of cationic monomer is usually at least 80 mole %, suitably 100%. Examples of suitable ethylenically unsaturated cationic monomers include dialkylaminoalkyl (meth)-acrylates and -acrylamides, preferably in quaternised form, and diallyl dialkyl ammonium chlorides, e.g. diallyl dimethyl ammonium chloride (DADMAC), preferably homopolymers and copolymers of DADMAC. The organic polymeric cationic coagulants usually have a molecular weight in the range of from 1,000 to 700,000, suitably from 10,000 to 500,000. Examples of suitable inorganic coagulants include aluminium compounds, e.g. alum and polyaluminium compounds, e.g. polyaluminium chlorides, polyaluminium sulphates, polyaluminium silicate sulphates and mixtures thereof.
The components of the drainage and retention aids according to the invention can be added to the stock in conventional manner and in any order. When using drainage and retention aids comprising a silica-based sol and organic polymer, it is preferred to add the organic polymer to the stock before adding the silica-based sol, even if the opposite order of addition may be used. It is further preferred to add the organic polymer before a shear stage, which can be selected from pumping, mixing, cleaning, etc., and to add the silica-based sol after that shear stage. When using a cationic coagulant, it is preferably added to the cellulosic suspension before the addition of the silica-based sol, preferably also before the addition of the organic polymer(s).
The components of the drainage and retention aids according to the invention are added to the stock to be dewatered in amounts which can vary within wide limits depending on, inter alia, type and number of components, type of furnish, filler content, type of filler, point of addition, etc. Generally the components are added in amounts that give better drainage and retention than is obtained when not adding the components. The silica-based sol is usually added in an amount of at least 0.001% by weight, often at least 0.005% by weight, calculated as SiO2 and based on dry furnish, i.e. dry cellulosic fibres and optional fillers, and the upper limit is usually 1.0% and suitably 0.5% by weight. The organic polymer is usually added in an amount of at least 0.001%, often at least 0.005% by weight, based on dry furnish, and the upper limit is usually 3% and suitably 1.5% by weight. When using a cationic polymeric coagulant, it can be added in an amount of at least 0.05%, based on dry furnish. Suitably, the amount is in the range of from 0.07 to 0.5%, preferably in the range from 0.1 to 0.35%. When using an aluminium compound as the inorganic coagulant, the total amount added is usually at least 0.05%, calculated as Al2O3 and based on dry furnish. Suitably the amount is in the range of from 0.1 to 3.0%, preferably in the range from 0.5 to 2.0%.
Further additives which are conventional in papermaking can of course be used in combination with the additives according to the invention, such as, for example, dry strength agents, wet strength agents, optical brightening agents, dyes, sizing agents like rosin-based sizing agents and cellulose-reactive sizing agents, e.g. alkyl and alkenyl ketene dimers and ketene multimers, alkyl and alkenyl succinic anhydrides, etc. The cellulosic suspension, or stock, can also contain mineral fillers of conventional types such as, for example, kaolin, china clay, titanium dioxide, gypsum, talc and natural and synthetic calcium carbonates such as chalk, ground marble and precipitated calcium carbonate.
The process of this invention is used for the production of paper. The term “paper”, as used herein, of course include not only paper and the production thereof, but also other cellulosic sheet or web-like products, such as for example board and paperboard, and the production thereof. The process can be used in the production of paper from different types of suspensions of cellulose-containing fibres and the suspensions should suitably contain at least 25% by weight and preferably at least 50% by weight of such fibres, based on dry substance. The suspension can be based on fibres from chemical pulp such as sulphate, sulphite and organosolv pulps, mechanical pulp such as thermomechanical pulp, chemothermomechanical pulp, refiner pulp and groundwood pulp, from both hardwood and softwood, and can also be based on recycled fibres, optionally from de-inked pulps, and mixtures thereof. The pH of the suspension, the stock, can be within the range of from about 3 to about 10. The pH is suitably above 3.5 and preferably within the range of from 4 to 9.
The invention is further illustrated in the following example which, however, is not intended to limit the same. Parts and % relate to parts by weight and % by weight, respectively, unless otherwise stated.
EXAMPLES
The following equipment and starting materials were used throughout the Examples:
    • (a) Reactor equipped with a stirrer;
    • (b) Ion exchange resin Amberlite® IRC84SP (available from Rohm & Haas) which was regenerated with sulphuric acid according to manufacturer's instruction;
    • (c) Aqueous sodium silicate solution having a SiO2 content of about 21 wt. % and mole ratio of SiO2 to Na2O of 3.32;
    • (d) Aqueous sodium aluminate solution containing 2.44 wt. % Al2O3;
    • (e) Aqueous choline hydroxide solution having a choline hydroxide content of 35 wt. %; and
    • (f) Aqueous sodium hydroxide solution having a concentration of 5 moles per kilo.
Example 1
This example illustrates the preparation of a silica-based sol according to the invention: Regenerated ion exchange resin (471 g) and water (1,252 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (298 g) was then added to the slurry at a rate of 5 g/min. After the addition of sodium silicate, the pH of the slurry was about 7.3. The slurry was then stirred for another 44 minutes, whereupon the pH of the aqueous phase was 6.9. Thereafter additional aqueous sodium silicate (487 g) was added to the slurry at a rate of 5 g/min. The obtained silica-based sol was separated from the ion exchange resin.
The obtained silica-based sol had the following properties: SiO2 content=8.6 wt. %; mole ratio Si:Na=11.0; pH=10.4; specific surface area=680 m2/g; and S-value=20%.
Example 2
This example illustrates the preparation of another silica-based sol according to the invention: Aqueous sodium aluminate (52 g) was added to the sol (527.4 g) according to Example 1 under vigorous stirring during a period of 10 min.
The obtained silica-based sol had the following properties: SiO2 content=7.7 wt. %; mole ratio Si:Na=7.5; mole ratio Si:Al=26.2; pH=10.7; specific surface area=790 m2/g; and S-value=18%.
Example 3
This example illustrates the preparation of yet another silica-based sol according to the invention: Aqueous choline hydroxide (7.9 g) was added to the sol (395 g) according to Example 1 under vigorous stirring at a rate of 4 g/min.
The obtained silica-based sol had the following properties: SiO2 content=8.4 wt. %; mole ratio Si:Na=11.1; mole ration Si:N=24.6; pH=10.8; specific surface area=890 m2/g; and S-value=18%.
Example 4
This example illustrates the preparation of still another silica-based sol according to the invention: Regenerated ion exchange resin (600 g) and water (1,600 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (764 g) was then added to the slurry at a rate of 6.8 g/min. After the addition of sodium silicate, the pH of the slurry was about 8, whereupon the ion exchange resin was separated from the aqueous phase. Aqueous sodium hydroxide (30 g) was added to the aqueous phase at the rate of 10 g/min.
The obtained silica-based sol had the following properties: SiO2 content=8.7 wt. %; mole ratio Si:Na=8.9; pH=10.6; specific surface area=810 m2/g; and S-value=25%.
Example 5
This example illustrates the preparation of another silica-based sol according to the invention: Aqueous sodium aluminate (83 g) was added to the sol (776 g) according to Example 4 under vigorous stirring during a period of 10 min.
The obtained silica-based sol had the following properties: SiO2 content=6.1 wt. %; mole ratio Si:Na=5.9; mole ratio Si:Al=20.3; pH=10.9; specific surface area=930 m2/g; and S-value=22%.
Example 6
This example illustrates the preparation of yet another silica-based sol according to the invention: Aqueous choline hydroxide (14.3 g) was added to the sol (714 g) according to Example 4 under vigorous stirring at a rate of 4 g/min.
The obtained silica-based sol had the following properties: SiO2 content=6.6 wt. %; mole ratio Si:Na=9.0; mole ration Si:N=18.9; pH=11; specific surface area=1,010 m2/g; and S-value=23%.
Example 7
This example illustrates the preparation of yet another silica-based sol according to the invention: Regenerated ion exchange resin (595 g) and water (1,605 g) were charged into a reactor. The obtained slurry was stirred vividly and heated to a temperature of 30° C. Aqueous sodium silicate (849 g) was then added to the slurry at a rate of 6.3 g/min. The slurry was then stirred for another 135 minutes, whereupon the pH of the aqueous phase was 7.9. Thereafter additional aqueous sodium silicate (326 g) was added to the slurry at a rate of 6.3 g/min. The obtained silica-based sol was separated from the ion exchange resin.
The obtained silica-based sol had the following properties: SiO2 content=9.3 wt. %; mole ratio Si:Na=7.5; pH=10.4; specific surface area=850 m2/g; and S-value=23%.
Example 8
The following silica-based sols, Ref. 1a to Ref. 3, were prepared for comparison purposes:
Ref. 1a is a silica-based sol prepared according to the disclosure of Example 4 of U.S. Pat. Nos. 6,372,089 and 6,372,806.
Ref. 1b is a silica-based sol prepared according to the general disclosure of column 4 of U.S. Pat. Nos. 6,372,089 and 6,372,806, wherein in step (c) the contents of the reaction vessel was stirred until the pH of the contents of the vessel was 9.2
Ref. 1c is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,447,604 which had an S-value of about 25%, a mole ratio of Si:Al of about 19 and contained silica particles with a specific surface area of about 900 m2/g SiO2.
Ref. 1d is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,603,805 with an S-value of 34% and contained silica particles with a specific surface area of about 700 m2/g.
Ref. 2a is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,368,833 which had an S-value of about 25%, a mole ratio of Si:Al of about 19 and contained silica particles with a specific surface area of about 900 m2/g SiO2 which were surface-modified with aluminium.
Ref. 2b is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 5,368,833 which had an S-value of 20%, a mole ratio of Si:Al of about 18 and contained silica particles with a specific surface area of about 820 m2/g SiO2 which were surface-modified with aluminium.
Ref. 3 is a silica-based sol prepared according to the disclosure of U.S. Pat. No. 6,379,500 which had an S-value of about 30%, mole ratio of Si:Na of about 10, mole ratio of Si:N of about 21, and contained choline hydroxide and silica particles with a specific surface area of about 900 m2/g SiO2.
Example 9
In the following tests, drainage performance of the silica-based sols according to Examples 1 to 3 (“Ex. 1”, “Ex. 2” and “Ex. 3”, respectively) were tested against the drainage performance of silica-based sols according to Example 8. The drainage performance was evaluated by means of a Dynamic Drainage Analyser (DDA), available from Akribi, Sweden, which measures the time for draining a set volume of stock through a wire when removing a plug and applying a vacuum to that side of the wire opposite to the side on which the stock is present.
The stock used was based on a standard fine paper furnish consisting of 60° A bleached birch sulfate and 40% bleached pine sulfate. 30% ground calcium carbonate was added to the stock as filler and 0.3 g/l of Na2SO4.10H2O was added to increase conductivity. Stock pH was 8.1, conductivity 1.5 mS/cm and consistency 0.5%. In the tests, the silica-based sols were tested in conjunction with a cationic polymer being cationic starch having a degree of substitution of about 0.042. The starch was added in an amount of 8 kg/tonne, calculated as dry starch on dry furnish.
The stock was stirred in a baffled jar at a speed of 1,500 rpm throughout the test and chemical additions to the stock were made as follows:
i) adding cationic starch followed by stirring for 30 seconds;
ii) adding silica-based sol followed by stirring for 15 seconds; and
iii) draining the stock while automatically recording the drainage time.
Tables 1 to 3 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO2 and based on dry furnish.
TABLE 1
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 1 Ref. 1a Ref. 1c
1 8 0 19.4 19.4 19.4
2 8 1.0 13.4 14.7 14.9
3 8 1.5 12.4 13.7 13.9
4 8 2.0 10.8 13.1 13.3
TABLE 2
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 2 Ref. 1a Ref. 2a
1 8 0 19.4 19.4 19.4
2 8 1.0 13.8 14.7 14.1
3 8 1.5 12.2 13.7 13.7
4 8 2.0 11.1 13.1 12.6
TABLE 3
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 3 Ref. 1a Ref. 3a
1 8 0 19.4 19.4 19.4
2 8 1.0 12.6 14.7 11.4
3 8 1.5 10.0 13.7 10.5
4 8 2.0 9.2 13.1 10.9
Example 10
The silica-based sols according to Examples 1 to 3 were further evaluated following the procedure of Example 9 except that a cationic polyacrylamide (“PAM”) was used instead of cationic starch. In addition, the stock was stirred in a baffled jar at a speed of 1,500 rpm throughout the test and chemical additions to the stock were made as follows:
i) adding cationic polyacrylamide followed by stirring for 20 seconds;
ii) adding silica-based sol followed by stirring for 10 seconds; and
iii) draining the stock while automatically recording the drainage time.
Tables 4 to 6 show the results obtained when using different dosages of cationic polyacrylamide, kg/tonne, calculated as dry starch on dry furnish, and silica-based sol, kg/tonne, calculated as SiO2 and based on dry furnish.
TABLE 4
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 1 Ref. 1a Ref. 1c
1 0.8 0 17.2 17.2 17.2
2 0.8 0.25 10.4 11.1 11.5
3 0.8 0.50 7.8 8.2 9.0
4 0.8 0.75 6.9 7.1 7.5
TABLE 5
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 2 Ref. 1a Ref. 2a
1 0.8 0 17.2 17.2 17.2
2 0.8 1.0 9.8 11.1 10.0
3 0.8 1.5 7.2 8.2 7.7
4 0.8 2.0 6.6 7.1 7.4
TABLE 6
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 3 Ref. 1a Ref. 3a
1 0.8 0 17.2 17.2 17.2
2 0.8 1.0 9.9 11.1 11.2
3 0.8 1.5 7.5 8.2 9.6
4 0.8 2.0 6.8 7.1 10.1
Example 11
The silica-based sols according to Examples 4 to 6 were tested against silica-based sols according to Example 8 following the procedure of Example 9.
Tables 7 to 9 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO2 and based on dry furnish.
TABLE 7
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 4 Ref. 1a Ref. 1d
1 8 0 20.6 20.6 20.6
2 8 1.0 14.6 15.5 15.1
3 8 1.5 13.3 14.1 14.4
4 8 2.0 12.4 13.6 13.4
TABLE 8
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 5 Ref. 1a Ref. 2a
1 8 0 20.6 20.6 20.6
2 8 1.0 13.9 15.5 14.7
3 8 1.5 12.8 14.1 13.6
4 8 2.0 12.5 13.6 13.5
TABLE 9
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 6 Ref. 1a Ref. 3
1 8 0 20.6 20.6 20.6
2 8 1.0 11.3 15.5 10.5
3 8 1.5 9.6 14.1 10.0
4 8 2.0 9.1 13.6 10.0
Example 12
The silica-based sols according to Examples 4 to 6 were tested against silica-based sols according to Example 8 following the procedure of Example 10.
Tables 10 to 12 show the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO2 and based on dry furnish.
TABLE 10
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 4 Ref. 1b Ref. 1c
1 0.8 0 16.0 16.0 16.0
2 0.8 0.25 9.5 10.8 10.7
3 0.8 0.50 6.9 8.1 8.0
4 0.8 0.75 6.0 7.8 7.1
TABLE 11
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 5 Ref. 2a Ref. 2b
1 0.8 0 16.0 16.0 16.0
2 0.8 0.25 8.6 9.1 8.7
3 0.8 0.50 6.6 7.9 7.4
4 0.8 0.75 6.0 7.6 7.2
TABLE 12
Cationic
PAM Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 6 Ref. 3
1 0.8 0 16.0 16.0
2 0.8 0.25 9.2 10.5
3 0.8 0.50 7.1 9.0
4 0.8 0.75 6.9 10.2
Example 13
The silica-based sol according to Example 7 was tested against a silica-based sol according to Example 8 following the procedure of Example 9.
Table 13 shows the results obtained when using varying dosages of silica-based sol, kg/tonne, calculated as SiO2 and based on dry furnish.
TABLE 13
Cationic
Starch Silica
Test Dosage Dosage Dewatering Time [s]
No. [kg/t] [kg/t] Ex. 7 Ref. 1b Ref. 1c
1 8 0 27.1 27.1 27.1
2 8 1.0 16.6 18.3 18.5
3 8 1.5 14.8 17.2 16.7
4 8 2.0 13.3 15.8 16.1

Claims (23)

1. A process for producing an aqueous silica-based sol containing aggregated silica-based particles which comprises:
(a) providing a reaction vessel equipped with means for stirring;
(b) adding to said reaction vessel:
(i) a cationic ion exchange resin having at least part of its ion exchange capacity in hydrogen form, and
(ii) an aqueous solution of alkali metal silicate, to form an aqueous slurry;
(c) stirring said aqueous slurry in said reaction vessel to allow particle aggregation and until the pH of the aqueous phase is in the range of from 5.0 to 8.0;
(d) adding one or more materials to the aqueous phase obtained after step (c) to form an aqueous phase having a pH of above 9.0; and
separating said ion exchange resin from the aqueous phase after step (c) or after step (d).
2. The process according to claim 1 wherein in step (c) the aqueous slurry is stirred until the pH of the aqueous phase is in the range of from 6.0 to 8.0.
3. The process according to claim 2 wherein in step (c) the aqueous slurry is stirred until the pH of the aqueous phase is in the range of from 6.5 to 7.5.
4. The process according to claim 1 wherein in step (c) the slurry is stirred to allow particle aggregation or microgel formation corresponding to an S-value in the range of from 4 to 45%.
5. The process according to claim 4 wherein the S-value is in the range of from 10 to 25%.
6. The process according to claim 1 wherein step (d) comprises adding an alkaline material.
7. The process according to claim 6 wherein the alkaline material is an aqueous alkali metal silicate.
8. The process according to claim 6 wherein the alkaline material is an aqueous alkali metal hydroxide.
9. The process according to claim 1 wherein step (d) comprises adding an organic nitrogen-containing compound.
10. The process according to claim 9 wherein the organic nitrogen-containing compound is choline hydroxide.
11. The process according to claim 1 wherein the aqueous solution of alkali metal silicate is added to the reaction vessel at a rate in the range of from 0.5 to 50 g SiO2 per minute and kg ion exchange resin, calculated as ion exchange resin having 100% of its ion exchange capacity in hydrogen form.
12. The process according to claim 11, wherein in step (b) said aqueous solution of alkali metal silicate is added to said reaction vessel at a rate in the range of from 2 to 20 g SiO2 per minute and kg ion exchange resin, calculated as ion exchange resin having 100% of its ion exchange capacity in hydrogen form.
13. The process according to claim 1 wherein in step (d) the pH of the aqueous phase is adjusted to be in the range of from about 9.5 to about 11.2.
14. The process according to claim 1 wherein step (d) comprises adding an aluminium compound.
15. The process according to claim 1 wherein in step (d) the pH of the aqueous phase is adjusted by first adding aqueous sodium silicate and subsequently adding aqueous sodium aluminate.
16. The process according to claim 1 wherein in step (d) the pH of the aqueous phase is adjusted by first adding an aqueous alkali metal silicate, then the ion exchange resin is separated from the aqueous phase and an aqueous aluminium compound is subsequently added to the obtained aqueous phase.
17. The process according to claim 1 wherein the silica-based sol obtained has an S-value is in the range of from 10 to 50%.
18. The process according to claim 1 wherein the silica-based sol obtained contains silica-based particles having a specific surface area from 700 to 950 m2/g.
19. An aqueous silica-based sol obtained by the process according to claim 1.
20. The process according to claim 1, wherein the aqueous solution of alkali metal silicate has a pH above 11.
21. The process according to claim 1, wherein the aqueous solution of alkali metal silicate has an SiO2 content of from about 15 to about 25% by weight.
22. The process according to claim 1, wherein the aqueous solution of alkali metal silicate has a molar ratio SiO2 to Na2O, K2O or Li2O, or a mixture thereof, in the range of from about 4.5:1 to 1.5:1.
23. A process for producing a silica-based sol containing aggregated silica-based particles which comprises: (a) providing a reaction vessel equipped with means for stirring; (b) adding to said reaction vessel: (i) a cationic ion exchange resin having at least part of the ion exchange capacity in hydrogen form, and (ii) an aqueous solution of alkali metal silicate having a pH above 11 and an SiO2 content of from about 15 to about 25% by weight, to form an aqueous slurry; (c) stirring said aqueous slurry in said reaction vessel to allow particle aggregation and until the pH of the aqueous phase is in the range of from 5.0 to 8.0; (d) adding one or more materials to the aqueous phase obtained after step (c) to form an aqueous phase having a pH of above 9.0; and (e) separating said ion exchange resin from the aqueous phase after step (c) or after step (d).
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US20110196047A1 (en) * 1999-05-04 2011-08-11 Akzo Nobel N.V. Silica-based sols

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Citations (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2577485A (en) 1950-09-08 1951-12-04 Du Pont Process of making stable silica sols and resulting composition
US2601352A (en) 1950-01-16 1952-06-24 Du Pont Silica sols and method of making same
US2630410A (en) 1949-04-19 1953-03-03 Union Carbide & Carbon Corp Nongelling aqueous silica sols stabilized with boron compounds
US2727008A (en) 1953-08-25 1955-12-13 Du Pont Process for increasing the concentration of a metastable silica sol
US2750345A (en) 1954-02-25 1956-06-12 Du Pont Process for producing sols of 5-8 millimicron silica particles, and product
US2754270A (en) 1952-05-07 1956-07-10 Exxon Research Engineering Co Process for the manufacture of silica hydrosols
US2892797A (en) 1956-02-17 1959-06-30 Du Pont Process for modifying the properties of a silica sol and product thereof
US2974108A (en) 1957-01-14 1961-03-07 Du Pont Aluminosilicate aquasols and their preparation
US3083167A (en) 1955-05-05 1963-03-26 Owens Corning Fiberglass Corp Manufacture and stabilization of colloidal silicic acid
US3374180A (en) 1964-12-28 1968-03-19 Monsanto Co Process for preparing silica aquasols
US3533816A (en) 1965-10-22 1970-10-13 Du Pont Preparation of high ratio alkali metal silicates
US3655578A (en) 1969-05-08 1972-04-11 Du Pont High surface area stabilized silica sols and process for preparing same
US3857925A (en) 1971-07-27 1974-12-31 Canadian Patents Dev Preparation of reinforcing amorphous silica
US3916058A (en) 1973-06-25 1975-10-28 Nalco Chemical Co Method of treating paper and textiles with organically modified sio' 2 'aquasols
US3956171A (en) 1973-07-30 1976-05-11 E. I. Du Pont De Nemours And Company Process for preparing stable positively charged alumina coated silica sols and product thereof
SU549541A1 (en) 1975-12-31 1977-03-05 Центральный научно-исследовательский институт бумаги Method of preparation of paper pulp
US4272409A (en) 1977-08-31 1981-06-09 E. I. Du Pont De Nemours And Company Aluminosilicate sols and powders
US4388150A (en) 1980-05-28 1983-06-14 Eka Aktiebolag Papermaking and products made thereby
WO1986000100A1 (en) 1984-06-07 1986-01-03 Eka Ab Papermaking process
WO1986005826A1 (en) 1985-04-03 1986-10-09 Eka Nobel Aktiebolag Papermaking process
US4750974A (en) 1986-02-24 1988-06-14 Nalco Chemical Company Papermaking aid
SU1446106A1 (en) 1987-07-01 1988-12-23 Армянский филиал Всесоюзного научно-исследовательского института химических реактивов и особо чистых химических веществ Method of producing alumosilicon sol
WO1989008741A1 (en) 1988-03-08 1989-09-21 Eka Nobel Ab A process for the production of paper
US4927498A (en) 1988-01-13 1990-05-22 E. I. Du Pont De Nemours And Company Retention and drainage aid for papermaking
US4954220A (en) 1988-09-16 1990-09-04 E. I. Du Pont De Nemours And Company Polysilicate microgels as retention/drainage aids in papermaking
US5100581A (en) 1990-02-22 1992-03-31 Nissan Chemical Industries Ltd. Method of preparing high-purity aqueous silica sol
US5127994A (en) 1988-05-25 1992-07-07 Eka Nobel Ab Process for the production of paper
US5176891A (en) 1988-01-13 1993-01-05 Eka Chemicals, Inc. Polyaluminosilicate process
US5230833A (en) 1989-06-09 1993-07-27 Nalco Chemical Company Low sodium, low metals silica polishing slurries
US5240561A (en) 1992-02-10 1993-08-31 Industrial Progress, Inc. Acid-to-alkaline papermaking process
WO1993024409A1 (en) 1992-05-26 1993-12-09 E.I. Du Pont De Nemours And Company Method for preparing low-concentration polysilicate microgels
WO1994005597A1 (en) 1992-09-02 1994-03-17 Exxon Chemical Patents Inc. Micro particles
US5368833A (en) 1989-11-09 1994-11-29 Eka Nobel Ab Silica sols having high surface area
WO1995023021A1 (en) 1994-02-28 1995-08-31 Eka Chemicals Ab Silica-based sols, preparation and use of the sols
US5447604A (en) 1989-11-09 1995-09-05 Eka Nobel Ab Silica sols, a process for the production of silica sols and use of the sols
US5470435A (en) 1994-03-14 1995-11-28 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5503820A (en) 1992-05-26 1996-04-02 E. I. Du Pont De Nemours And Company Method for preparing low-concentration polysilicate microgels
US5543014A (en) 1994-03-14 1996-08-06 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5571494A (en) 1995-01-20 1996-11-05 J. M. Huber Corporation Temperature-activated polysilicic acids
US5603805A (en) 1992-08-31 1997-02-18 Eka Nobel, Ab Silica sols and use of the sols
US5626721A (en) 1994-03-14 1997-05-06 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5707494A (en) 1994-03-14 1998-01-13 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5708069A (en) 1997-02-24 1998-01-13 Dow Corning Corporation Method for making hydrophobic silica gels under neutral conditions
US5846384A (en) 1995-06-15 1998-12-08 Eka Chemicals Ab Process for the production of paper
WO1998056715A1 (en) 1997-06-09 1998-12-17 Akzo Nobel N.V. Polysilicate microgels
WO1998056716A1 (en) 1997-06-09 1998-12-17 Akzo Nobel N.V. Polysilicate microgels and silica-based materials
US5964693A (en) 1992-06-03 1999-10-12 Bayer Aktiengesellschaft Continuous preparation of silica sols which contain large particles
US6083997A (en) 1998-07-28 2000-07-04 Nalco Chemical Company Preparation of anionic nanocomposites and their use as retention and drainage aids in papermaking
WO2000066492A1 (en) 1999-05-04 2000-11-09 Akzo Nobel N.V. Silica-based sols
US6228217B1 (en) 1995-01-13 2001-05-08 Hercules Incorporated Strength of paper made from pulp containing surface active, carboxyl compounds
US6372806B1 (en) 1998-03-06 2002-04-16 Nalco Chemical Company Method of making colloidal silica
US6379500B2 (en) 1999-12-20 2002-04-30 Akzo Nobel Nv Silica-based sols
US20020139502A1 (en) 1998-04-27 2002-10-03 Hans Hallstrom Process for the production of paper
US20030024671A1 (en) 1999-05-04 2003-02-06 Michael Persson Silica-based sols
US7629392B2 (en) * 2004-04-07 2009-12-08 Akzo Nobel N.V. Silica-based sols and their production and use
US7732495B2 (en) * 2004-04-07 2010-06-08 Akzo Nobel N.V. Silica-based sols and their production and use

Patent Citations (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2630410A (en) 1949-04-19 1953-03-03 Union Carbide & Carbon Corp Nongelling aqueous silica sols stabilized with boron compounds
US2601352A (en) 1950-01-16 1952-06-24 Du Pont Silica sols and method of making same
US2577485A (en) 1950-09-08 1951-12-04 Du Pont Process of making stable silica sols and resulting composition
US2754270A (en) 1952-05-07 1956-07-10 Exxon Research Engineering Co Process for the manufacture of silica hydrosols
US2727008A (en) 1953-08-25 1955-12-13 Du Pont Process for increasing the concentration of a metastable silica sol
US2750345A (en) 1954-02-25 1956-06-12 Du Pont Process for producing sols of 5-8 millimicron silica particles, and product
US3083167A (en) 1955-05-05 1963-03-26 Owens Corning Fiberglass Corp Manufacture and stabilization of colloidal silicic acid
US2892797A (en) 1956-02-17 1959-06-30 Du Pont Process for modifying the properties of a silica sol and product thereof
US2974108A (en) 1957-01-14 1961-03-07 Du Pont Aluminosilicate aquasols and their preparation
US3374180A (en) 1964-12-28 1968-03-19 Monsanto Co Process for preparing silica aquasols
US3533816A (en) 1965-10-22 1970-10-13 Du Pont Preparation of high ratio alkali metal silicates
US3655578A (en) 1969-05-08 1972-04-11 Du Pont High surface area stabilized silica sols and process for preparing same
US3857925A (en) 1971-07-27 1974-12-31 Canadian Patents Dev Preparation of reinforcing amorphous silica
US3916058A (en) 1973-06-25 1975-10-28 Nalco Chemical Co Method of treating paper and textiles with organically modified sio' 2 'aquasols
US3956171A (en) 1973-07-30 1976-05-11 E. I. Du Pont De Nemours And Company Process for preparing stable positively charged alumina coated silica sols and product thereof
SU549541A1 (en) 1975-12-31 1977-03-05 Центральный научно-исследовательский институт бумаги Method of preparation of paper pulp
US4272409A (en) 1977-08-31 1981-06-09 E. I. Du Pont De Nemours And Company Aluminosilicate sols and powders
US4388150A (en) 1980-05-28 1983-06-14 Eka Aktiebolag Papermaking and products made thereby
WO1986000100A1 (en) 1984-06-07 1986-01-03 Eka Ab Papermaking process
WO1986005826A1 (en) 1985-04-03 1986-10-09 Eka Nobel Aktiebolag Papermaking process
US4750974A (en) 1986-02-24 1988-06-14 Nalco Chemical Company Papermaking aid
SU1446106A1 (en) 1987-07-01 1988-12-23 Армянский филиал Всесоюзного научно-исследовательского института химических реактивов и особо чистых химических веществ Method of producing alumosilicon sol
US4927498A (en) 1988-01-13 1990-05-22 E. I. Du Pont De Nemours And Company Retention and drainage aid for papermaking
US5176891A (en) 1988-01-13 1993-01-05 Eka Chemicals, Inc. Polyaluminosilicate process
WO1989008741A1 (en) 1988-03-08 1989-09-21 Eka Nobel Ab A process for the production of paper
US5127994A (en) 1988-05-25 1992-07-07 Eka Nobel Ab Process for the production of paper
US4954220A (en) 1988-09-16 1990-09-04 E. I. Du Pont De Nemours And Company Polysilicate microgels as retention/drainage aids in papermaking
US5230833A (en) 1989-06-09 1993-07-27 Nalco Chemical Company Low sodium, low metals silica polishing slurries
US5368833A (en) 1989-11-09 1994-11-29 Eka Nobel Ab Silica sols having high surface area
US5447604A (en) 1989-11-09 1995-09-05 Eka Nobel Ab Silica sols, a process for the production of silica sols and use of the sols
US5100581A (en) 1990-02-22 1992-03-31 Nissan Chemical Industries Ltd. Method of preparing high-purity aqueous silica sol
US5240561A (en) 1992-02-10 1993-08-31 Industrial Progress, Inc. Acid-to-alkaline papermaking process
WO1993024409A1 (en) 1992-05-26 1993-12-09 E.I. Du Pont De Nemours And Company Method for preparing low-concentration polysilicate microgels
US5279807A (en) 1992-05-26 1994-01-18 E. I. Du Pont De Nemours And Company Method for preparing low-concentration polysilicate microgels
US5503820A (en) 1992-05-26 1996-04-02 E. I. Du Pont De Nemours And Company Method for preparing low-concentration polysilicate microgels
US5964693A (en) 1992-06-03 1999-10-12 Bayer Aktiengesellschaft Continuous preparation of silica sols which contain large particles
US5603805A (en) 1992-08-31 1997-02-18 Eka Nobel, Ab Silica sols and use of the sols
WO1994005597A1 (en) 1992-09-02 1994-03-17 Exxon Chemical Patents Inc. Micro particles
WO1995023021A1 (en) 1994-02-28 1995-08-31 Eka Chemicals Ab Silica-based sols, preparation and use of the sols
US5543014A (en) 1994-03-14 1996-08-06 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5482693A (en) 1994-03-14 1996-01-09 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5626721A (en) 1994-03-14 1997-05-06 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5707494A (en) 1994-03-14 1998-01-13 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US5470435A (en) 1994-03-14 1995-11-28 E. I. Du Pont De Nemours And Company Process for preparing water soluble polyaluminosilicates
US6228217B1 (en) 1995-01-13 2001-05-08 Hercules Incorporated Strength of paper made from pulp containing surface active, carboxyl compounds
US5571494A (en) 1995-01-20 1996-11-05 J. M. Huber Corporation Temperature-activated polysilicic acids
US5846384A (en) 1995-06-15 1998-12-08 Eka Chemicals Ab Process for the production of paper
US5708069A (en) 1997-02-24 1998-01-13 Dow Corning Corporation Method for making hydrophobic silica gels under neutral conditions
WO1998056715A1 (en) 1997-06-09 1998-12-17 Akzo Nobel N.V. Polysilicate microgels
WO1998056716A1 (en) 1997-06-09 1998-12-17 Akzo Nobel N.V. Polysilicate microgels and silica-based materials
US6372089B1 (en) 1998-03-06 2002-04-16 Nalco Chemical Company Method of making paper
US6372806B1 (en) 1998-03-06 2002-04-16 Nalco Chemical Company Method of making colloidal silica
US20020139502A1 (en) 1998-04-27 2002-10-03 Hans Hallstrom Process for the production of paper
US6083997A (en) 1998-07-28 2000-07-04 Nalco Chemical Company Preparation of anionic nanocomposites and their use as retention and drainage aids in papermaking
WO2000066491A1 (en) 1999-05-04 2000-11-09 Akzo Nobel N.V. Silica-based sols
WO2000066492A1 (en) 1999-05-04 2000-11-09 Akzo Nobel N.V. Silica-based sols
US20030024671A1 (en) 1999-05-04 2003-02-06 Michael Persson Silica-based sols
US6379500B2 (en) 1999-12-20 2002-04-30 Akzo Nobel Nv Silica-based sols
US7629392B2 (en) * 2004-04-07 2009-12-08 Akzo Nobel N.V. Silica-based sols and their production and use
US7732495B2 (en) * 2004-04-07 2010-06-08 Akzo Nobel N.V. Silica-based sols and their production and use

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
Derwent abstract No. 008026336, abstract of SU 1446106.
English language translation of SU 1446106.
European Search Report, EP 04044 5049 dated Aug. 25, 2004.
George W. Sears Jr., "Determination of Specific Surface Area of Colloidal Silica by Titration with Sodium Hydroxide," Grasselli Chemicals Department and E.I. Du Pont de Nemours and Co. Inc., Dec. 12, 1956, vol. 28, pp. 1981-1983.
International Search Report, PCT Application No. PCT/SE2005/000489, dated Sep. 13, 2005.
R.K. Iler et al., "Degree of Hydration of Particles of Colloidal Silica in Aqueous Solution," Grasselli Chemicals Department and E.I. Du Pont de Nemours and Co. Inc., Jan. 16, 1956, vol. 60, pp. 955-957.
Robert H. Moffett, "On-site Production of a Silica-based Microparticulate Retention and Drainage Aid," Tappi Journal, vol. 77, No. 12, pp. 133-138.
V. Rieman, et al., "Ion-exchange chromatography in analytical chemistry," Moscow, Mir Publishing House, 1973, pp. 86-88.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110196047A1 (en) * 1999-05-04 2011-08-11 Akzo Nobel N.V. Silica-based sols
US8835515B2 (en) * 1999-05-04 2014-09-16 Akzo Nobel, N.V. Silica-based sols

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